Tel:
Fax:
Email:
Creative Biolabs

Genetic Anxiety Mouse Model Development Service

Are you currently facing long development cycles, poor translatability of hits, and the complexity of genetic anxiety research? Our genetic anxiety mouse models development services help you accelerate target validation and de-risk your drug pipeline through CRISPR/Cas9 and conditional gene editing under stringent methodological controls.

Genetic Anxiety Mouse Models Development Services. The complexity of anxiety, a severe and heterogeneous psychiatric illness, necessitates the use of genetically defined animal models to ensure translational fidelity in drug discovery. Gene knockout (KO) and Knock-in (KI) technology is essential for dissecting the molecular pathways underlying these disorders. Cited literature confirms the vital role of the Serotonergic and HPA Axis systems as high-impact targets for modeling human anxiety.

Workflow Advantages Available Models Offerings Related Services FAQs

How Genetic Anxiety Mouse Models Development Services Can Assist Your Project?

We provide comprehensive, end-to-end solutions that move beyond simply creating a genetic alteration. Our services deliver fully validated preclinical models optimized for high-throughput screening and mechanistic dissection of anxiety pathways.

Discover How We Can Help - Request a Consultation

Workflow of our Genetic Anxiety Mouse Models Development Services. (Creative Biolabs Original)

Workflow: From Target to Translational Model

Required Starting Materials
  1. Target Gene Identification: The official gene symbol and desired genetic alteration (e.g., GABAAα2H101R point mutation, or LoxP insertion flanking Exon 3).
  2. Specific Mouse Strain Background: Selection of the required genetic background (e.g.,C57BL/6N) to control for known background-related phenotypic variability.
  3. Project Scope and Timing: Defined cohort sizes and experimental milestones.
Final Deliverables
  1. Project-Ready Mice: F1 or F2 Heterozygous/Homozygous mice for the target line.
  2. Genetic Validation Report: Comprehensive gRNA/Vector Design, NGS sequencing data confirming F0 and germline transmission status.
  3. Baseline Behavioral Validation Report: Data on the anxiety-like phenotype (e.g., open arm time, center-to-periphery ratio) compared to wildtype controls.

Why Choose Us?

Our leadership in genetic anxiety mouse model development is based on over two decades of experience, ensuring your research is powered by models that possess maximum construct validity and translational relevance.

Key Advantages and Unique Features:

  • Superior Conditional Gene Editing: We specialize in utilizing Cre-Lox systems to generate Conditional Knockout (cKO) models, addressing the critical issue of developmental compensation that plagues constitutive KO. This ensures you study adult gene function, not embryonic adaptations.
  • Rigorous Phenotypic Control: Our validation protocols mandate a multi-assay battery (EPM, OFT, Light-Dark Box, CO2 Panic Test), controlling for confounding factors like non-specific locomotor activity to confirm a genuine anxiety-related phenotype.
  • Mastery of Critical Pathways: Our established expertise with the Serotonergic (SERT, 5-HT1A) and HPA Axis (CRH-R1, GR) systems provides pre-optimized strategies for the most relevant targets in neuropsychiatry.

Genetic Anxiety Mouse Models

The creation of genetically precise mouse models is the most powerful tool for elucidating the molecular pathology of human anxiety. We leverage the inherent genetic tractability of the mouse to model clinically relevant conditions with high fidelity.

The Imperative of Genetic Precision in Anxiety Modeling

The complexity of anxiety pathology—involving multiple interacting neural circuits and distinct neurochemical systems—demands models where the genetic variables are meticulously controlled. Our focus is on models that achieve true construct validity, ensuring the underlying biological mechanism driving the anxiety-like phenotype in the mouse faithfully reflects the human disease etiology.

This focus allows our clients to:

  • Dissect Specific Pathways: Investigate the precise role of single nucleotide polymorphisms (SNPs), non-coding RNAs, or specific gene-protein interactions (e.g., in the hippocampus, amygdala, or prefrontal cortex) implicated by human Genome-Wide Association Studies (GWAS). We focus on high-impact targets within the Serotonergic system (e.g., SERT, 5-HT1A), the HPA axis (CRH,CRH-R1), and Neurotrophin signaling (e.g., BDNF).
  • Explore QTL Regions: Target genes within quantitative trait loci (QTL) regions, such as the distal end of mouse chromosome 1 (syntenic with human 1q22−q32), which have been consistently linked to multiple anxiety-related traits.
  • Validate Novel Targets: Move beyond broad anxiolytic screens to validate drug candidates against specific, human-relevant genetic targets, vastly improving the predictability of Phase I and II trials.

The Gold Standard in Behavioral Phenotyping

Model generation is only half the equation; the other half is validation. Our anxiety model validation packages employ industry-standard, ethologically based behavioral assays designed for reproducibility and sensitivity to both classical and non-BDZ anxiolytics.

Core Anxiety and Activity Assays:

  • Elevated Plus-Maze (EPM) & Zero Maze: Measures innate anxiety via the conflict between exploration and aversion to open/elevated spaces.
  • Open Field Test (OFT): Quantifies general activity, exploration, and emotionality (measured by time spent in the center vs. periphery).
  • Light-Dark Box: Assesses avoidance behavior based on novelty and aversion to bright illumination.
  • Carbon Dioxide (Panic) Test: Used for highly specific screening of panic-like responses, such as the innate freezing reaction to elevated CO2.

Commitment to Methodological Rigor:

To ensure the translational power of your data, all behavioral assessments are conducted under strict conditions, featuring:

  • Blinding and Randomization: Strict technician blinding to genotype and treatment groups, paired with randomized testing procedures to mitigate experimental bias.
  • Sex-Specific Analysis: Consideration of sex as an independent variable, acknowledging divergent behavioral and pharmacological sensitivities between male and female cohorts, which is crucial for diseases with observed sex differences.
  • Environmental Consistency: Meticulous control of lighting, noise, temperature, and circadian timing across all testing sessions to guarantee maximum data reliability.

What We Can Offer?

This section details the specific, high-value models and services offered by CBL, designed for precise mechanistic studies and target validation in complex anxiety disorders. We ensure every model maximizes construct validity by focusing on key neurotransmitter systems and disease mechanisms.

  • Customized Genetic Model Design: CBL provides design and delivery of fully customized KO, KI, and Humanized models for any anxiety-related gene, regardless of pathway complexity or genomic location.
  • Precision CRISPR/Cas9 Editing: Utilization of next-generation CRISPR/Cas9 technology for targeted genome manipulation, guaranteeing high on-target efficiency and minimized off-target risk, a cornerstone of reliable preclinical research.
  • Conditional Gene Regulation Systems: Expertise in Cre-Lox Conditional KO systems, enabling temporal and tissue-specific gene deletion to definitively eliminate developmental compensation effects and study gene function in adult neural circuits.
  • Focused Pathway Model Libraries: Immediate access to pre-validated models across critical anxiety neurochemical systems, including Serotonergic (5-HT1A, SERT), HPA Axis (CRH-R1, CRH-R2), and GABAA subunits (α1, α2 ,α3).
  • Rigorous Multi-Dimensional Phenotyping: Inclusion of a comprehensive behavioral assay battery (EPM, OFT, Light-Dark Box, CO2 Panic Test) in the validation process to confirm a genuine anxiety-like phenotype, minimizing locomotor confounding variables.
  • Translational Genetic Backgrounds: Provision of models on defined, controlled genetic backgrounds (e.g., C57BL/6N) with full genetic and phenotypic documentation to maximize cross-laboratory reproducibility and translatability.

Related Services

To fully leverage your custom Genetic Anxiety Mouse Model, CBL offers complementary services designed to accelerate your preclinical pipeline:

FAQs

Q Why should I choose a Conditional KO model over a simple Constitutive KO for my anxiety research?

A Constitutive KO removes the gene from the first cell stage, potentially triggering developmental compensation that masks the true adult function. Conditional KO allows you to inactivate the gene at a specific developmental stage or in a specific brain region (e.g., the amygdala), providing definitive data on the gene's function in the adult, uncompensated neural circuit.

Q How do you ensure my anxiety-like phenotype is not simply due to locomotor or motor impairment?

A Every anxiety model we validate is subjected to the Open Field Test (OFT) as a primary control for general locomotor activity. We carefully analyze activity parameters (distance moved, rearing) alongside anxiety metrics (EPM open arm time). A valid anxiety model must show changes in emotionality metrics without significant, confounding changes in basal activity.

For more information and to discuss how our services can meet your specific project requirements, please contact our team of experts.

Contact Our Team for More Information and to Discuss Your Project.

For Research Use Only. Not For Clinical Use.
In Vivo Services
Hot Products
Fill out this form for a quote Inquiry Form Send Inquiry
USA

Tel:

Fax:

Email:

UK

Tel:

Email:

Germany

Tel:

Email:

Inquiry Basket
compare

Send inquiry